Canonical Allele Identifier: CA2123464658

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415832C= , CM000676.2:g.23415832C= GRCh38
NC_000014.8:g.23885041C= , CM000676.1:g.23885041C= GRCh37
NC_000014.7:g.22954881C= NCBI36
NG_007884.1:g.24830G= , LRG_384:g.24830G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4954G= (MYH7) MANE Select ENSP00000347507.3:p.Asp1652=
ENST00000355349.3:c.4954G= (MYH7) ENSP00000347507.3:p.Asp1652=
NM_000257.3:c.4954G= (MYH7) NP_000248.2:p.Asp1652=
NR_126491.1:n.261+3C= (MHRT)
XM_017021340.1:c.4954G= (MYH7) XP_016876829.1:p.Asp1652=
NM_000257.4:c.4954G= (MYH7) MANE Select NP_000248.2:p.Asp1652=